Phase 2 Lymphoma Trial, Recruiting NCT06554561 Sponsor: Second Affiliated Hospital, School of Medicine, Zhejiang University Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT06554561
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who have been diagnosed with a specific type of lymphoma called CD20-positive diffuse large B-cell lymphoma (DLBCL), confirmed by a tissue test
  • People whose lymphoma is only present in the central nervous system — meaning the brain, spinal cord, eyes, or the lining around the brain and spinal cord
  • People where tests including scans and a bone marrow test have confirmed the lymphoma has not spread to any other part of the body
  • People who have not previously received chemotherapy or radiation therapy (a small, short course of a steroid called dexamethasone at low doses for fewer than 5 days may be acceptable — confirm with trial site)
  • People aged 18 to 75 years (inclusive)
  • People with a general health and activity level rated between 0 and 3 on a standard medical scale (this covers people who are fully active through to people who are capable of limited self-care — confirm with trial site)
  • People who have at least one measurable area of lymphoma that is 1.0 cm or larger, as seen on a specialised brain scan (enhanced MRI)
  • People expected to live for at least 3 months, in the opinion of the treating doctor
  • People who are willing and able to read and sign a consent form
  • People who are able to attend follow-up visits on schedule and communicate well with the research team throughout the trial
  • Women who could become pregnant must agree to use highly effective contraception during treatment and for 6 months after the last dose; men who are sexually active must also agree to use highly effective contraception during treatment and for 6 months after the last dose

Who may not be able to join:

  • People whose lymphoma has spread to parts of the body outside the central nervous system
  • People who have previously received chemotherapy, radiation therapy, or a stem cell transplant
  • People who have or have had another cancer that currently requires active treatment
  • People who have a chronic or currently active infection requiring ongoing antibiotic, antifungal, or antiviral treatment (infections with a virus called EBV may be an exception — confirm with trial site)
  • People with uncontrolled heart or blood vessel disease, bleeding disorders, clotting disorders, or connective tissue diseases
  • People with other uncontrolled health conditions that the research team considers unsuitable for participation
  • People whose blood test results at the start of the trial fall outside acceptable ranges — including low counts of white blood cells, neutrophils (a type of immune cell), platelets, or haemoglobin, or abnormally high levels of certain liver or kidney markers (unless these are caused by the lymphoma itself — confirm with trial site)
  • People with active hepatitis B infection, active hepatitis C infection, HIV, or other inherited or acquired immune deficiency conditions (people with certain hepatitis B markers may still be considered if specific virus level tests come back below a set threshold — confirm with trial site)
  • People who are pregnant or currently breastfeeding
  • People with a history of drug use or substance abuse
  • People with a mental illness or any condition that may make it difficult to fully follow the study requirements
  • People with a known allergy to the trial drug or any of its ingredients
  • People who are unable to swallow capsules, or who have a condition that seriously affects how their digestive system absorbs or processes food and medication, such as removal of the stomach or small intestine, or a complete bowel blockage
  • People who are unable to have an enhanced MRI scan
  • People considered unsuitable for the trial for any other reason, at the discretion of the research team

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 6 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Phone: +8613989883884

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Registry
ClinicalTrials.gov
Start date
31 August 2024
Est. completion
31 August 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

MTD; Objective response rate(ORR)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 6 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov